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帕金森病中的p38丝裂原活化蛋白激酶和磷脂酰肌醇-3激酶/蛋白激酶B信号级联反应

p38 MAPK and PI3K/AKT Signalling Cascades inParkinson's Disease.

作者信息

Jha Saurabh Kumar, Jha Niraj Kumar, Kar Rohan, Ambasta Rashmi K, Kumar Pravir

机构信息

Molecular Neuroscience and Functional Genomics Laboratory, Department of Biotechnology, Delhi Technological University (Formerly DCE), Delhi, India.

Molecular Neuroscience and Functional Genomics Laboratory, Department of Biotechnology, Delhi Technological University (Formerly DCE), Delhi, India. ; Department of Neurology, Tufts University School of Medicine, Boston, MA (USA).

出版信息

Int J Mol Cell Med. 2015 Spring;4(2):67-86.

Abstract

Parkinson's disease (PD) is a chronic neurodegenerative condition which has the second largest incidence rate among all other neurodegenerative disorders barring Alzheimer's disease (AD). Currently there is no cure and researchers continue to probe the therapeutic prospect in cell cultures and animal models of PD. Out of the several factors contributing to PD prognosis, the role of p38 MAPK (Mitogen activated protein-kinase) and PI3K/AKT signalling module in PD brains is crucial because the impaired balance between the pro- apoptotic and anti-apoptotic pathways trigger unwanted phenotypes such as microglia activation, neuroinflammation, oxidative stress and apoptosis. These factors continue challenging the brain homeostasis in initial stages thereby essentially assisting the dopaminergic (DA) neurons towards progressive degeneration in PD. Neurotherapeutics against PD shall then be targeted against the misregulated accomplices of the p38 and PI3K/AKT cascades. In this review, we have outlined many such established mechanisms involving the p38 MAPK and PI3K/AKT pathways which can offer therapeutic windows for the rectification of aberrant DA neuronal dynamics in PD brains.

摘要

帕金森病(PD)是一种慢性神经退行性疾病,在除阿尔茨海默病(AD)之外的所有其他神经退行性疾病中发病率排名第二。目前尚无治愈方法,研究人员继续在PD的细胞培养和动物模型中探索治疗前景。在导致PD预后的几个因素中,p38丝裂原活化蛋白激酶(MAPK)和PI3K/AKT信号模块在PD大脑中的作用至关重要,因为促凋亡和抗凋亡途径之间的平衡受损会引发小胶质细胞活化、神经炎症、氧化应激和凋亡等不良表型。这些因素在疾病初期持续挑战大脑的稳态,从而实质上促使多巴胺能(DA)神经元在PD中进行性退化。针对PD的神经治疗应针对p38和PI3K/AKT级联反应中失调的相关因素。在这篇综述中,我们概述了许多涉及p38 MAPK和PI3K/AKT途径的既定机制,这些机制可为纠正PD大脑中异常的DA神经元动态提供治疗窗口。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b69/4499569/338d4beb4a49/ijmcm-4-067-g001.jpg

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